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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77389Erstellt: 24. Oktober 2026

Water → 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one

https://huagongshe.com/de/reaction/77389

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl-4-nitrobenzenesulfonateHCID 22582—
EduktSodium hydrideHCID 24758—
Edukt7-bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-oneHCID 69928893—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-oneHCID 6992854850,2%

Reaktionsschritte

7-Bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-one (Intermediate 23A) (0.1 g, 0.299 mmol) was dissolved in THF (4 mL), under an atmosphere of nitrogen. Sodium hydride (0.018 g, 0.448 mmol) was added and reaction stirred for 30 minutes. The reaction was then cooled using an ice bath and methyl 4-nitrobenzenesulfonate (0.065 g, 0.299 mmol) was added. The reaction was allowed to warm to room temperature and left to stir overnight. Water was added to the reaction mixture and extracted with EtOAC (×2). The organics were combined and washed with brine, dried (MgSO4) filtered and concentrated under reduced pressure. The mixture was purified on silica (25 g column on Isolera 4) eluting with 0-10% methanol in dichloromethane to afford 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one (51 mg, 0.15 mmol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841289B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d964deca7655450c9db475cc20959061
Quellennotizuspto-grants-2014_09